HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104353Generated: November 1, 2026
Water → rac-tert-butyl N-((1R,2R)-2-aminocyclopentyl)carbamate
https://huagongshe.com/reaction/2104353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | Cyclopentane-1,2-diamine | HCID 243938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | rac-tert-butyl N-((1R,2R)-2-aminocyclopentyl)carbamate | HCID 17040217 | 98.5% |
Reaction Steps
(±)-trans-1,2-Cyclopentanediamine (WO98/30574) (692 mg) was dissolved in methylene chloride (10 mL), and to the solution were added triethylamine (1.1 mL) and 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (493 mg) at 0° C., followed by stirring at 0° C. for 1 hour. Subsequently, additional 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (493 mg) was added thereto, and the thus-obtained mixture was stirred at room temperature for 7 hours. Water was added to the reaction mixture to partition the mixture. The organic layer was washed with saturated brine, and was dried over sodium sulfate anhydrate. The residue was purified by silica gel flash column chromatography (methylene chloride:methanol=9:1), to thereby give the title compound (395 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576135B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-bebed518f25a460696381fb45085a585 |
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| Source note | uspto-grants-2009_08 |
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